The Crucial Role of Polymorphonuclear Leukocytes in Resistance to Salmonella dublin Infections in Genetically Susceptible and Resistant Mice
Macrophages are considered to be the mediators of resistance to extra-intestinal Salmonella infections. Nevertheless, the initial cellular response to Salmonella infections consists primarily of polymorphonuclear leukocytes (PMN). To determine whether PMN serve an important function for the infected...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 1998-06, Vol.95 (13), p.7676-7681 |
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description | Macrophages are considered to be the mediators of resistance to extra-intestinal Salmonella infections. Nevertheless, the initial cellular response to Salmonella infections consists primarily of polymorphonuclear leukocytes (PMN). To determine whether PMN serve an important function for the infected host, we made mice neutropenic with the rat mAb to RB6-8C5 and infected them i.v. with ≈ 103Salmonella dublin or an isogenic derivative that lacks the virulence plasmid (LD842). We infected BALB/c mice, which have a point mutation in the macrophage-expressed gene Nramp1 that makes them susceptible to Salmonella, and BALB/c.D2 congenic mice, which have the wild-type Nramp1 gene that makes them resistant to Salmonella. Both mouse strains were resistant to LD842, and neutropenia made only the BALB/c strain susceptible to this infection. Neutropenic congenic mice, however, were susceptible only to wild-type S. dublin (plasmid+). These results show a complex interplay between plasmid-virulence genes in Salmonella, host macrophages, and PMN. Mice with normal macrophages need PMN to defend against nontyphoid Salmonella that carry a virulence plasmid but not against Salmonella without virulence plasmids. Mice with a mutant Nramp1 gene need PMN to defend against all Salmonella, even those that lack virulence plasmids. These results, plus the evidence that PMN kill Salmonella efficiently in vitro, suggest that Salmonella have adapted to grow inside macrophages where they are relatively sheltered from PMN. The adaptations that allow Salmonella to survive in macrophages do not protect them from PMN. |
doi_str_mv | 10.1073/pnas.95.13.7676 |
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Nevertheless, the initial cellular response to Salmonella infections consists primarily of polymorphonuclear leukocytes (PMN). To determine whether PMN serve an important function for the infected host, we made mice neutropenic with the rat mAb to RB6-8C5 and infected them i.v. with ≈ 103Salmonella dublin or an isogenic derivative that lacks the virulence plasmid (LD842). We infected BALB/c mice, which have a point mutation in the macrophage-expressed gene Nramp1 that makes them susceptible to Salmonella, and BALB/c.D2 congenic mice, which have the wild-type Nramp1 gene that makes them resistant to Salmonella. Both mouse strains were resistant to LD842, and neutropenia made only the BALB/c strain susceptible to this infection. Neutropenic congenic mice, however, were susceptible only to wild-type S. dublin (plasmid+). These results show a complex interplay between plasmid-virulence genes in Salmonella, host macrophages, and PMN. Mice with normal macrophages need PMN to defend against nontyphoid Salmonella that carry a virulence plasmid but not against Salmonella without virulence plasmids. Mice with a mutant Nramp1 gene need PMN to defend against all Salmonella, even those that lack virulence plasmids. These results, plus the evidence that PMN kill Salmonella efficiently in vitro, suggest that Salmonella have adapted to grow inside macrophages where they are relatively sheltered from PMN. The adaptations that allow Salmonella to survive in macrophages do not protect them from PMN.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.95.13.7676</identifier><identifier>PMID: 9636209</identifier><language>eng</language><publisher>United States: National Academy of Sciences of the United States of America</publisher><subject>Alleles ; Animals ; Antibodies, Monoclonal - immunology ; Bacteria ; Biological Sciences ; Carrier Proteins - genetics ; Carrier Proteins - immunology ; Cation Transport Proteins ; Genetic Predisposition to Disease ; Genetics ; Humans ; Immunity, Innate - genetics ; Infections ; Leukocytes ; Liver ; Macrophages ; Macrophages - immunology ; Membrane Proteins - genetics ; Membrane Proteins - immunology ; Mice ; Mice, Inbred BALB C ; Mice, Inbred DBA ; Neutropenia ; Neutropenia - complications ; Neutropenia - immunology ; Neutrophils ; Neutrophils - immunology ; Plasmids ; Rats ; Salmonella ; Salmonella Infections, Animal - complications ; Salmonella Infections, Animal - genetics ; Salmonella Infections, Animal - immunology ; Spleen ; Virulence</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1998-06, Vol.95 (13), p.7676-7681</ispartof><rights>Copyright 1993-1998 National Academy of Sciences</rights><rights>Copyright National Academy of Sciences Jun 23, 1998</rights><rights>1998</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c477t-40c9ebd74cdb49d4fab2362edd5fc1f8eb099d6d74613534b41b87e7892cc4713</citedby><cites>FETCH-LOGICAL-c477t-40c9ebd74cdb49d4fab2362edd5fc1f8eb099d6d74613534b41b87e7892cc4713</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/95/13.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/45263$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/45263$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,723,776,780,799,881,27901,27902,53766,53768,57992,58225</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9636209$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vassiloyanakopoulos, Antonis P.</creatorcontrib><creatorcontrib>Okamoto, Sharon</creatorcontrib><creatorcontrib>Fierer, Joshua</creatorcontrib><title>The Crucial Role of Polymorphonuclear Leukocytes in Resistance to Salmonella dublin Infections in Genetically Susceptible and Resistant Mice</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Macrophages are considered to be the mediators of resistance to extra-intestinal Salmonella infections. Nevertheless, the initial cellular response to Salmonella infections consists primarily of polymorphonuclear leukocytes (PMN). To determine whether PMN serve an important function for the infected host, we made mice neutropenic with the rat mAb to RB6-8C5 and infected them i.v. with ≈ 103Salmonella dublin or an isogenic derivative that lacks the virulence plasmid (LD842). We infected BALB/c mice, which have a point mutation in the macrophage-expressed gene Nramp1 that makes them susceptible to Salmonella, and BALB/c.D2 congenic mice, which have the wild-type Nramp1 gene that makes them resistant to Salmonella. Both mouse strains were resistant to LD842, and neutropenia made only the BALB/c strain susceptible to this infection. Neutropenic congenic mice, however, were susceptible only to wild-type S. dublin (plasmid+). These results show a complex interplay between plasmid-virulence genes in Salmonella, host macrophages, and PMN. Mice with normal macrophages need PMN to defend against nontyphoid Salmonella that carry a virulence plasmid but not against Salmonella without virulence plasmids. Mice with a mutant Nramp1 gene need PMN to defend against all Salmonella, even those that lack virulence plasmids. These results, plus the evidence that PMN kill Salmonella efficiently in vitro, suggest that Salmonella have adapted to grow inside macrophages where they are relatively sheltered from PMN. The adaptations that allow Salmonella to survive in macrophages do not protect them from PMN.</description><subject>Alleles</subject><subject>Animals</subject><subject>Antibodies, Monoclonal - immunology</subject><subject>Bacteria</subject><subject>Biological Sciences</subject><subject>Carrier Proteins - genetics</subject><subject>Carrier Proteins - immunology</subject><subject>Cation Transport Proteins</subject><subject>Genetic Predisposition to Disease</subject><subject>Genetics</subject><subject>Humans</subject><subject>Immunity, Innate - genetics</subject><subject>Infections</subject><subject>Leukocytes</subject><subject>Liver</subject><subject>Macrophages</subject><subject>Macrophages - immunology</subject><subject>Membrane Proteins - genetics</subject><subject>Membrane Proteins - immunology</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred DBA</subject><subject>Neutropenia</subject><subject>Neutropenia - complications</subject><subject>Neutropenia - immunology</subject><subject>Neutrophils</subject><subject>Neutrophils - immunology</subject><subject>Plasmids</subject><subject>Rats</subject><subject>Salmonella</subject><subject>Salmonella Infections, Animal - complications</subject><subject>Salmonella Infections, Animal - genetics</subject><subject>Salmonella Infections, Animal - immunology</subject><subject>Spleen</subject><subject>Virulence</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFks1uEzEUhUcIVNLCGgkJZLGAVVL_zXgssUERlEpBoLasLY_nDnFw7NT2oOYdeGgcEkWFBay8ON859rm-VfWM4BnBgp1vvE4zWc8Im4lGNA-qCcGSTBsu8cNqgjEV05ZT_rg6TWmFMZZ1i0-qE9mwhmI5qX7eLAHN42isdugqOEBhQF-C265D3CyDH40DHdECxu_BbDMkZD26gmRT1t4AygFda7cOHpzTqB87V_RLP4DJNvjf9AV4yNZo57boekwGNtl25SLt-2NSRp-sgSfVo0G7BE8P51n19cP7m_nH6eLzxeX83WJquBB5yrGR0PWCm77jsueD7mipA31fD4YMLXRYyr4pQENYzXjHSdcKEK2kpiQQdla93eduxm4NvQGfo3ZqE-1ax60K2qo_FW-X6lv4oSgVFBf764M9htsRUlZrW2qVAXgIY1JCyprSuv0vSBpOeNvWBXz1F7gKY_RlBopiwkTLJC3Q-R4yMaQUYTg-mGC1Wwa1WwYla0WY2i1Dcby43_PIH36_6C8P-s54VO8HvPknoIbRuQx3uZDP9-Qq5RCPKK9pw9gvhRXVMg</recordid><startdate>19980623</startdate><enddate>19980623</enddate><creator>Vassiloyanakopoulos, Antonis P.</creator><creator>Okamoto, Sharon</creator><creator>Fierer, Joshua</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><general>National Academy of Sciences</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19980623</creationdate><title>The Crucial Role of Polymorphonuclear Leukocytes in Resistance to Salmonella dublin Infections in Genetically Susceptible and Resistant Mice</title><author>Vassiloyanakopoulos, Antonis P. ; Okamoto, Sharon ; Fierer, Joshua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c477t-40c9ebd74cdb49d4fab2362edd5fc1f8eb099d6d74613534b41b87e7892cc4713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Alleles</topic><topic>Animals</topic><topic>Antibodies, Monoclonal - immunology</topic><topic>Bacteria</topic><topic>Biological Sciences</topic><topic>Carrier Proteins - genetics</topic><topic>Carrier Proteins - immunology</topic><topic>Cation Transport Proteins</topic><topic>Genetic Predisposition to Disease</topic><topic>Genetics</topic><topic>Humans</topic><topic>Immunity, Innate - genetics</topic><topic>Infections</topic><topic>Leukocytes</topic><topic>Liver</topic><topic>Macrophages</topic><topic>Macrophages - immunology</topic><topic>Membrane Proteins - genetics</topic><topic>Membrane Proteins - immunology</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred DBA</topic><topic>Neutropenia</topic><topic>Neutropenia - complications</topic><topic>Neutropenia - immunology</topic><topic>Neutrophils</topic><topic>Neutrophils - immunology</topic><topic>Plasmids</topic><topic>Rats</topic><topic>Salmonella</topic><topic>Salmonella Infections, Animal - complications</topic><topic>Salmonella Infections, Animal - genetics</topic><topic>Salmonella Infections, Animal - immunology</topic><topic>Spleen</topic><topic>Virulence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vassiloyanakopoulos, Antonis P.</creatorcontrib><creatorcontrib>Okamoto, Sharon</creatorcontrib><creatorcontrib>Fierer, Joshua</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vassiloyanakopoulos, Antonis P.</au><au>Okamoto, Sharon</au><au>Fierer, Joshua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Crucial Role of Polymorphonuclear Leukocytes in Resistance to Salmonella dublin Infections in Genetically Susceptible and Resistant Mice</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1998-06-23</date><risdate>1998</risdate><volume>95</volume><issue>13</issue><spage>7676</spage><epage>7681</epage><pages>7676-7681</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Macrophages are considered to be the mediators of resistance to extra-intestinal Salmonella infections. Nevertheless, the initial cellular response to Salmonella infections consists primarily of polymorphonuclear leukocytes (PMN). To determine whether PMN serve an important function for the infected host, we made mice neutropenic with the rat mAb to RB6-8C5 and infected them i.v. with ≈ 103Salmonella dublin or an isogenic derivative that lacks the virulence plasmid (LD842). We infected BALB/c mice, which have a point mutation in the macrophage-expressed gene Nramp1 that makes them susceptible to Salmonella, and BALB/c.D2 congenic mice, which have the wild-type Nramp1 gene that makes them resistant to Salmonella. Both mouse strains were resistant to LD842, and neutropenia made only the BALB/c strain susceptible to this infection. Neutropenic congenic mice, however, were susceptible only to wild-type S. dublin (plasmid+). These results show a complex interplay between plasmid-virulence genes in Salmonella, host macrophages, and PMN. Mice with normal macrophages need PMN to defend against nontyphoid Salmonella that carry a virulence plasmid but not against Salmonella without virulence plasmids. Mice with a mutant Nramp1 gene need PMN to defend against all Salmonella, even those that lack virulence plasmids. These results, plus the evidence that PMN kill Salmonella efficiently in vitro, suggest that Salmonella have adapted to grow inside macrophages where they are relatively sheltered from PMN. The adaptations that allow Salmonella to survive in macrophages do not protect them from PMN.</abstract><cop>United States</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>9636209</pmid><doi>10.1073/pnas.95.13.7676</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alleles Animals Antibodies, Monoclonal - immunology Bacteria Biological Sciences Carrier Proteins - genetics Carrier Proteins - immunology Cation Transport Proteins Genetic Predisposition to Disease Genetics Humans Immunity, Innate - genetics Infections Leukocytes Liver Macrophages Macrophages - immunology Membrane Proteins - genetics Membrane Proteins - immunology Mice Mice, Inbred BALB C Mice, Inbred DBA Neutropenia Neutropenia - complications Neutropenia - immunology Neutrophils Neutrophils - immunology Plasmids Rats Salmonella Salmonella Infections, Animal - complications Salmonella Infections, Animal - genetics Salmonella Infections, Animal - immunology Spleen Virulence |
title | The Crucial Role of Polymorphonuclear Leukocytes in Resistance to Salmonella dublin Infections in Genetically Susceptible and Resistant Mice |
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